期刊
HIPPOCAMPUS
卷 22, 期 4, 页码 656-669出版社
WILEY
DOI: 10.1002/hipo.20935
关键词
estradiol; hippocampus; memory; transcription; synaptogenesis
资金
- NIA NIH HHS [R01 AG014979, R56 AG037984, AG036800, AG037984, R01 AG037984, R37 AG036800, AG14979, P30 AG028740] Funding Source: Medline
This review presents evidence for the idea that the expression of estrogen receptor alpha and beta (ERa and ER beta) interacts with the level of estradiol (E2) to influence the etiology of age-related cognitive decline and responsiveness to E2 treatments. There is a nonmonotonic dose response curve for E2 influences on behavior and transcription. Evidence is mounting to indicate that the dose response curve is shifted according to the relative expression of ERa and ER beta. Recent work characterizing age-related changes in the expression of ERa and ER beta in the hippocampus, as well as studies using mutant mice, and viral mediated delivery of estrogen receptors indicate that an age-related shift in ERa/ER beta expression, combined with declining gonadal E2 can impact transcription, cell signaling, neuroprotection, and neuronal growth. Finally, the role of ERa/ER beta on rapid E2 signaling and synaptogenesis as it relates to hippocampal aging is discussed. (c) 2011 Wiley Periodicals, Inc.
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